Enhancing Sensitivity in Low-Load Proteomics Orbitrap Workflows via SLIM Integration

A Structures for Lossless Ion Manipulation-Orbitrap Exploris 480 (SLIM-OE) ion mobility mass spectrometry (IM-MS) platform was developed, integrating SLIM IM separation with Orbitrap MS analysis. A "staggered IMS" mode was designed to acquire IM-<i>m</i>/<i>z</i> two-dimensional heatmap data via direct infusion for method development, and an LC compatible SLIM-enabled data-independent acquisition (SLIM-DIA) workflow was implemented for low sample load proteomics analysis. The study evaluated IM separation across a broad <i>m</i>/<i>z</i> range of ions and demonstrated up to a 190× sensitivity enhancement in both IM-MS and IM-MS/MS modes of operation relative to operation in MS and MS/MS modes, respectively. The increased sensitivity improved protein coverage for the Qual/Quant QC Mix proteins. Compared to standard DIA, SLIM-DIA achieved a 2.3× increase in protein group identification from 2 ng of HeLa on the modified instrument, while maintaining quantitative capabilities. This research highlights the potential of the SLIM-OE IM-MS system to enhance proteomics analysis, providing a foundation for future high-performance SLIM-Orbitrap instrumentation development.

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Publication Details

Journal
Analytical Chemistry
Published
2025-06-11
DOI
https://doi.org/10.1021/acs.analchem.5c00897
Citations
1
Primary Topic
Advanced Proteomics Techniques and Applications
Type
article
Field-Weighted Citation Impact
0.76
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Enhancing Sensitivity in Low-Load Proteomics Orbitrap Workflows via SLIM Integration

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Enhancing Sensitivity in Low-Load Proteomics Orbitrap Workflows via SLIM Integration

Alexander Makarov, Lukas Reiter, Oliver M. Bernhardt, Kyle L. Fort, Daniel DeBord, Jean‐Jacques Dunyach, Tobias P. Wörner, Brian Adamson, Alan McKenzie‐Coe, Roland Bruderer, Tejas Gandhi, Liulin Deng, Eloy R. Wouters
article en
1 citations

Abstract

A Structures for Lossless Ion Manipulation-Orbitrap Exploris 480 (SLIM-OE) ion mobility mass spectrometry (IM-MS) platform was developed, integrating SLIM IM separation with Orbitrap MS analysis. A "staggered IMS" mode was designed to acquire IM-<i>m</i>/<i>z</i> two-dimensional heatmap data via direct infusion for method development, and an LC compatible SLIM-enabled data-independent acquisition (SLIM-DIA) workflow was implemented for low sample load proteomics analysis. The study evaluated IM separation across a broad <i>m</i>/<i>z</i> range of ions and demonstrated up to a 190× sensitivity enhancement in both IM-MS and IM-MS/MS modes of operation relative to operation in MS and MS/MS modes, respectively. The increased sensitivity improved protein coverage for the Qual/Quant QC Mix proteins. Compared to standard DIA, SLIM-DIA achieved a 2.3× increase in protein group identification from 2 ng of HeLa on the modified instrument, while maintaining quantitative capabilities. This research highlights the potential of the SLIM-OE IM-MS system to enhance proteomics analysis, providing a foundation for future high-performance SLIM-Orbitrap instrumentation development.

Analytical ChemistryVol. 97(24)
Biognosys (Switzerland) (CH), Thermo Fisher Scientific (United States) (US), Thermo Fisher Scientific (Germany) (DE)
Openalex Percentile: Top 30%
Advanced Proteomics Techniques and Applications
0.76
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